NRBP1 and TSC22D proteins affect distal convoluted tubule physiology through modulation of the WNK pathway

The with-no-lysine (K) (WNK) kinases regulate processes such as cell volume and epithelial ion transport through the modulation of cation chloride cotransporters such as the NaCl cotransporter (NCC) present in the distal convoluted tubule (DCT) of the kidney. Recently, the interaction of WNKs with nuclear receptor binding protein 1 (NRBP1) and transforming growth factor-β-stimulated clone 22 domain (TSC22D) proteins was reported. Here, we explored the effect of NRBP1 and TSC22Ds on WNK signaling in vitro and in the DCT. TSC22D1.1, TSC22D2, and NRBP1 are localized in DCT WNK bodies, which are cytoplasmic biomolecular condensates associated with WNK activation. In HEK293 cells, long TSC22D isoforms and NRBP1 increase WNK4 activity. DCT-specific NRBP1-knockout mice have reduced NCC phosphorylation and activate a compensatory response. Thus, NRBP1 and long TSC22D proteins are positive modulators of WNK signaling and modulate Na<sup>+</sup> reabsorption in the kidney. NRBP1 and TSC22Ds likely influence WNK signaling in other tissues, affecting various physiological processes.

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Publication Details

Journal
Science Advances
Published
2025-07-16
DOI
https://doi.org/10.1126/sciadv.adv2083
Citations
2
Primary Topic
Ion Transport and Channel Regulation
Type
article
Field-Weighted Citation Impact
1.61

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article

NRBP1 and TSC22D proteins affect distal convoluted tubule physiology through modulation of the WNK pathway

Alejandro López‐Saavedra, Brenda Marquina‐Castillo, Germán Magaña-Ávila, María Castañeda‐Bueno et al.
2 citations
Science Advances
Ion Transport and Channel Regulation
1.61
article

NRBP1 and TSC22D proteins affect distal convoluted tubule physiology through modulation of the WNK pathway

Alejandro López‐Saavedra, Brenda Marquina‐Castillo, Germán Magaña-Ávila, María Castañeda‐Bueno, David H. Ellison, Toby A. Dite, Dario R. Alessi, Gerardo Gamba, Eréndira Rojas‐Ortega, Ramchandra V. Amnekar, Norma Vázquez, Eric J. Delpire, Héctor Carbajal‐Contreras, Michelle Téllez-Sütterlin, Kevin García-Ávila
article en
2 citations

Abstract

The with-no-lysine (K) (WNK) kinases regulate processes such as cell volume and epithelial ion transport through the modulation of cation chloride cotransporters such as the NaCl cotransporter (NCC) present in the distal convoluted tubule (DCT) of the kidney. Recently, the interaction of WNKs with nuclear receptor binding protein 1 (NRBP1) and transforming growth factor-β-stimulated clone 22 domain (TSC22D) proteins was reported. Here, we explored the effect of NRBP1 and TSC22Ds on WNK signaling in vitro and in the DCT. TSC22D1.1, TSC22D2, and NRBP1 are localized in DCT WNK bodies, which are cytoplasmic biomolecular condensates associated with WNK activation. In HEK293 cells, long TSC22D isoforms and NRBP1 increase WNK4 activity. DCT-specific NRBP1-knockout mice have reduced NCC phosphorylation and activate a compensatory response. Thus, NRBP1 and long TSC22D proteins are positive modulators of WNK signaling and modulate Na<sup>+</sup> reabsorption in the kidney. NRBP1 and TSC22Ds likely influence WNK signaling in other tissues, affecting various physiological processes.

Science AdvancesVol. 11(29)
Oregon Health & Science University (US), University of Dundee (GB), Vanderbilt University (US), Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán (MX), MRC Protein Phosphorylation and Ubiquitylation Unit (GB), VA Portland Health Care System (US), Instituto Nacional de Cancerología (MX), Universidad Nacional Autónoma de México (MX), Tecnológico de Monterrey (MX)
GlaxoSmithKline, Northwestern University, University of Dundee, Merck KGaA, Instituto Nacional de Cancerología, Fondation Leducq, Universidad Nacional Autónoma de México, Medical Research Council
Openalex Percentile: Top 16%
Ion Transport and Channel Regulation
1.61
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